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Clinical Trials/NCT04474093
NCT04474093
Completed
Not Applicable

Monolithic CAD/CAM Single Tooth Crowns Made From Different Ceramics: One Year Preliminary Results of a Randomized Clinical Trial

Hacettepe University0 sites36 target enrollmentAugust 24, 2016

Overview

Phase
Not Applicable
Intervention
Not specified
Conditions
Crowns (MeSH Unique ID: D003442), Single Tooth
Sponsor
Hacettepe University
Enrollment
36
Primary Endpoint
Survival rate and success (changes over time)
Status
Completed
Last Updated
5 years ago

Overview

Brief Summary

With the development of Computer Aided Design and Computer Aided manufacturing (CAD / CAM) systems, all ceramic restorations have been used with high success rates during the past 30 years in order to eliminate the disadvantages of metal ceramic restorations. Based on these developments, in every passing days new ceramic materials has been added to dental market. The aim of the present study was evaluating clinical results of single-tooth ceramic crowns in the posterior region produced from three different monolithic ceramic materials.

Registry
clinicaltrials.gov
Start Date
August 24, 2016
End Date
November 2018
Last Updated
5 years ago
Study Type
Interventional
Study Design
Parallel
Sex
All

Investigators

Responsible Party
Principal Investigator
Principal Investigator

Diler Deniz

Clinical Instructor, Prosthetic Dentistry

Hacettepe University

Eligibility Criteria

Inclusion Criteria

  • 18 years old
  • Individuals who have signed the informed consent form
  • Periodontally stable patients
  • Having devital teeth need to be restored in the posterior region
  • Having natural dentition or minimally invasive restoration against the restored tooth.

Exclusion Criteria

  • Diagnosed patients with temporomandibular joint problems
  • Insufficient supportive tooth tissue for restoration

Outcomes

Primary Outcomes

Survival rate and success (changes over time)

Time Frame: 1 year (Baseline to 12 months)

12 crowns were made from each group of three different ceramics: ZRGC, LDGC and RIGC. Thereafter, the restorations was evaluated in terms of any failure or loss of the restoration at any follow-up (6th and 12th months) periods. The results were obtained proportionally in percent (%).

Prosthetic evaluation changes

Time Frame: 1 year (Baseline to 12 months)

As recorded at the baseline (0), each restoration was assessed according to the modified the United States Public Health Service (USPHS) Ryge Criteria for prosthetic evaluation by a calibrated prosthodontics.USPHS criteria is based on the following ratings: Color match (Alpha,Bravo, Charlie), cavosurface marginal discoloration (Alpha,Bravo, Charlie), secondary caries (Alpha,Bravo), anatomic contour (Alpha,Bravo, Charlie), marginal integrity (Alpha,Bravo, Charlie), surface texture (Alpha,Bravo, Charlie) and gross fracture (Alpha,Bravo, Charlie).

Periodontal evaluation changes

Time Frame: 1 year (Baseline to 12 months)

Probing depth(PD): Probing depth is defined as the distance from the free gingival margin to the bottom of the periodontal pocket (mm). Clinical attachment level(CAL): The loss of CAL were measured and calculated by measuring recession and subtracting the periodontal probing depth (mm). Gingival bleeding time index(GBTI): The probe were swiped at apical portion of the gingival crevice from line angle interproximally and after 10 seconds assessed if there was bleeding or no bleeding on the mesial and distal (unit/tooth). Plaque index(PI, according to Silness and Löe, 1964): The total mean PI is the sum of the individual scores divided by the number of investigated sites. The thickness and extension of plaque were assessed (unit/tooth). Gingival index(GI, according to Löe, 1967): The total mean GI is the sum of the individual scores divided by the number of investigated sites. The GI for each tooth is the sum of the 4 individual scores divided by 4 (unit/tooth).

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